Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 18
rs1131691003
TP53
0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691042
TP53
0.752 0.360 17 7675052 splice donor variant C/T snv 12
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs1555525012
TP53
0.882 0.200 17 7673603 missense variant G/A snv 3
rs17884306
TP53
0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs121912661
TP53
1.000 0.120 17 7676264 missense variant C/A;G snv 1
rs77038344
TNS4
1.000 0.120 17 40487962 intron variant C/T snv 8.4E-02 1
rs78417682
TNS3
0.925 0.120 7 47449305 intron variant G/C snv 0.15 2
rs73328514
TNS3
1.000 0.120 7 47448971 intron variant A/T snv 0.15 1
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs4927850
TFRC
0.925 0.120 3 196024759 intron variant T/C snv 0.71 2